FIG 1 - uploaded by Michael Yabsley
Content may be subject to copyright.
Photographs of U.S. triatomine species, Triatoma and Paratriatoma. The image size relative to the scale bar represents the average length of each species. Photographs for T. incrassata , T. recurva , and P. hirsuta were unavailable . All photographs are by S. Kjos. 

Photographs of U.S. triatomine species, Triatoma and Paratriatoma. The image size relative to the scale bar represents the average length of each species. Photographs for T. incrassata , T. recurva , and P. hirsuta were unavailable . All photographs are by S. Kjos. 

Source publication
Article
Full-text available
Chagas' disease is caused by the protozoan parasite Trypanosoma cruzi and causes potentially life-threatening disease of the heart and gastrointestinal tract. The southern half of the United States contains enzootic cycles of T. cruzi, involving 11 recognized triatomine vector species. The greatest vector diversity and density occur in the western...

Context in source publication

Context 1
... initiatives (220, 269). Serological screening of blood components for T. cruzi is now compulsory in all but one of the countries in Latin America where the disease is endemic, and the prevalence of infection in screened donors has decreased substantially (196, 269). Nevertheless, Chagas’ disease screening coverage by country was estimated to vary from 25% to 100% in 2002, and the risk of transmission, though much decreased, has not been eliminated (269). The residual risk in Latin America where screening has been implemented is estimated to be 1:200,000 units (269, 308). Organ-derived transmission. Uninfected recipients who re- ceive an organ from a T. cruzi -infected donor may develop acute T. cruzi infection. However, transmission is not universal; in a series of 16 uninfected recipients of kidneys from infected donors, only 3 (19%) acquired T. cruzi infection (238). Nine- teen instances of transmission by organ transplantation have been documented in the literature (13 kidney, 1 kidney and pancreas, 3 liver, and 2 heart transplants) (16, 61, 66, 79, 99, 101, 157, 238, 279). The risk from heart transplantation is thought to be higher than that from kidney or liver transplantation (65). One case of transmission through unrelated cord blood transplantation has been reported (104). Oral transmission. Recently, increasing attention has focused on the oral route of T. cruzi transmission; several outbreaks attributed to contaminated fruit or sugar cane juice have been reported from Brazil and Venezuela (28, 82, 208). Most outbreaks are small, often affecting family groups in the Amazon region, where the palm fruit a ̧aí is a dietary staple that appears to be particularly vulnerable to contamination, perhaps from infected vectors living in the trees themselves (74, 208). The largest reported outbreak to date led to more than 100 infections among students and staff at a school in Caracas; locally prepared guava juice was implicated (82). The epidemiology of vector-borne T. cruzi is closely linked to the biological and ecological characteristics of local vectors and mammalian reservoir hosts. Triatomines of both sexes must take blood meals to develop through their nymphal stages to adults, and females require a blood meal to lay eggs. Thus, nymphs and adults of either sex may be infected with T. cruzi , but infection rates increase with increasing vector stage and age. Most domestic triatomine species feed nocturnally and are able to complete their blood meal without waking the host (169). The major Latin American vectors defecate during or immediately after taking a blood meal. T. cruzi infection is transmitted to wild mammals by sylvatic triatomine species; these bugs often colonize the nests of ro- dent or marsupial reservoir hosts (169, 311). Sylvatic triatomine adults may fly into human dwellings because of attraction by light and cause sporadic human infections (74). Domestic transmission cycles occur where vectors have become adapted to living in human dwellings and nearby animal enclosures; domestic mammals such as dogs, cats, and guinea pigs play important roles as triatomine blood meal sources and T. cruzi reservoir hosts (69, 124, 131). Some triatomine species can infest both domestic and sylvatic sites and may play a bridging role (192). There are more than 130 triatomine species in the Americas, many of which can be infected by and transmit T. cruzi (169, 311). However, a small number of highly domiciliated vectors are of disproportionate importance in the human epidemiology of disease (Table 2) (311). The domestic environment provides abundant blood meal sources, and poor quality housing with adobe or unfinished brick walls provides crevices and other diurnal hiding places for triatomines (170, 201). Thatch roofs provide an attractive habitat for some species (117). In communities where the disease is endemic, 25 to 100% of houses may be infested, and a house and its immediate sur- roundings may support large colonies of juvenile and adult bugs (170, 201, 230). In areas of the Amazon where deforestation and human immigration have occurred, tree-dwelling sylvatic triatomine populations have survived and rebounded by adapting to new vertebrate host species (2). These opportunistic vertebrates (opossums and rodents) are competent Chagas’ disease reservoirs and are acclimated to living in close proximity to humans where remnant vegetation is located. The concentration of triatomines and vertebrate reservoirs in the peridomestic realm has lead to increased interactions between sylvatic triatomine species and humans in deforested areas of the Amazon and Panama and to an apparent increase in the incidence of Chagas’ disease in humans (4, 244). Eleven species of triatomine bugs have been reported from the United States: Triatoma gerstaeckeri , T. incrassata , T. indictiva , T. lecticularia , T. neotomae , T. protracta , T. recurva , T. rubida , T. rubrofasciata , T. sanguisuga , and Paratriatoma hirsuta (Fig. 1 and Table 3). Triatomines are present across the southern half of the country, distributed from the Pacific to Atlantic coasts (Fig. 2). One species ( T. rubrofasciata ) is found in Hawaii. A high degree of polymorphism has been noted in several species across their geographic ranges, particularly T. protracta , T. rubida , and T. sanguisuga , resulting in proposed subspecies classifications (249, 251, 254, 296). However, due to the recognition of morphological intermediates across some subspecies groups and the absence of supporting data (e.g., paired molecular and morphological studies), these subspecies have not been universally accepted as valid taxonomic groups (110, 169). All U.S. species except T. rubrofasciata and T. sanguisuga have been collected in Mexico; the distribution of T. sanguisuga likely extends into northeastern Mexico as well (255). A review of the published literature from 1939 to 2010 resulted in reports of wild-caught triatomine bugs from 262 counties in 28 states. The greatest species diversity occurs in the southwest, particularly Texas, Arizona, and New Mexico. More specifically, high species diversity is concentrated in south-central Arizona and southwestern Texas, where up to five species have been recorded in a single county (Fig. 2). T. cruzi -infected specimens have been reported from 10 states, predominantly from counties in the Southwest (Fig. 3A). All species except T. incrassata and P. hirsuta have been found naturally infected with T. cruzi (Fig. 3B to L). County-level maps (Fig. 2 and 3) reflect in part where collection efforts have been focused over the past 70 years. There is no evidence of a temporal or spatial trend in the published reports to suggest any recent migration of species into or within the United States. The county maps do not necessarily reflect triatomine population densities or provide a complete representation of their distributions. Rather, the maps more likely provide an indication of where the bugs have been considered a pest to humans or animals and where field efforts were concentrated as a consequence or where specimens were collected coincidentally by researchers studying other animal systems (i.e., reports based on museum specimens). Collection records are more comprehensive in the southwestern states and Florida, with sparse records in the southeastern states. Early discovery of the association of U.S. triatomine bugs with Neotoma species of woodrats may have aided field research in the southwestern states, because woodrat species in this region build easily identifiable, above-ground dens. The absence of records in some areas of the southeastern United States may reflect a paucity of field studies or published records in those locations rather than being an indication of true absence of the bug. The detection of T. cruzi -infected wild mammals in many of these areas suggests the presence of the vectors. Additionally, recent efforts to model the geographic distribution of U.S. species based on the land cover, climate, and host composition of known collection sites indicate favorable habitat suitability in many of these unsurveyed or underreported regions (26, 137, 158, 259). Characteristics of each species are summarized in Table 3 and described in detail in the sections that follow. Triatoma gerstaeckeri (Stål). T. gerstaeckeri is one of the most frequently collected and tested species in the United States; 57.7% (1,038/1,800) of tested specimens were found to harbor T. cruzi . T. cruzi -infected specimens have been found in both Texas and New Mexico and in the majority of the counties where testing has been reported (Fig. 3B). Published reports from the 1930s to 1960s describe T. gerstaeckeri as a pest species of humans and livestock; the adult bugs were frequent invaders of rural houses in Texas, and reports of humans being bitten were common (217, 330, 332). Human encounters have been less frequently reported in recent decades (49, 151). Infected T. gerstaeckeri specimens were recently recovered from the residence of a child with acute Chagas’ disease in southern Texas (151). In northeastern Mexico, this species is considered an important Chagas’ disease vector due to its close association with human dwellings (184, 288). U.S. T. gerstaeckeri data derive predominantly from Texas, where the bug has been found in a wide variety of habitats. The species was collected from a rock squirrel burrow in a cave in the southeastern corner of New Mexico (341). Triatoma incrassata Usinger. T. incrassata is somewhat similar to T. protracta in size and general appearance of legs and head, but it has a distinctive abdominal margin which is largely yellow on the dorsal surface and entirely yellow on the ventral surface. It has been collected at lights in the two southern Arizona counties of Santa Cruz and Pima (Fig. 3C) (169, 255). The major mammalian hosts and T. cruzi infection prevalence for this species are unknown. Triatoma indictiva ...

Citations

... It affects humans in trypomastigote stage through its vector, the reduviid bugs, which suck blood from the host and help in transmitting the parasite by the deposition of the parasite loaded faeces on the host body surface. It can also be transmitted blood transfusion and organ transfusion (Bern et al., 2011;Schmunis, 2007). trans-[Ru(NO)(NH 3 ) 4 (isn)] 3+ (Fig. 3F) and trans-[Ru(NO)(NH 3 ) 4 (imN)] 3+ (Fig. 3G) complexes forming ...
Article
Full-text available
Background There are many infectious diseases in the world caused by parasites. Among them, toxoplasmosis, American trypanosomiasis, African trypanosomiasis, leishmaniasis, neosporosis and malaria are more common and contribute to a majority of the affected individuals. Main body Due to extensive use of antibiotics, antibiotic resistant strain of the parasites has developed. So, we need to develop a new metal ligand complexes which have many configurations, can overcome this drug resistance and also show significant results in elimination of the parasites. A series of anti-parasitic drugs have been formulated and tested for its activity. In this review, we have tried to see the interaction of different ruthenium drugs (arene ruthenium complex, ruthenium clotrimazole complex, etc.) on different parasites associated with the aforementioned diseases. Conclusion Combination of ruthenium to any organic ligand shows synergistic effects against parasite either by overcoming the drug resistance of the parasite or by binding with new targets due to the presence of ruthenium ion. The multiple modes of action generate an effective drug exhibiting anti-parasitic activity at low concentration. Graphical abstract
... About 20 million individuals are afflicted with this parasitic illness, which is mostly found in the tropical regions of Central and South America. Furthermore, the majority of those affected in Central America are immigrants from endemic parts of Latin America (3). T. cruzi, the parasite that causes Chagas disease, is thought to infect 6-7 million individuals globally (4). ...
... The migratory pathogens may now infiltrate cells, infect prey vectors, and start fresh replication cycles. If effective antitrypanosomal medication is not administered, the mammalian host remains infected for the duration of its life (3). ...
Article
Full-text available
Introduction Trypanosoma cruzi is a protozoan parasite that causes the tropical ailment known as Chagas disease, which has its origins in South America. Globally, it has a major impact on health and is transported by insect vector that serves as a parasite. Given the scarcity of vaccines and the limited treatment choices, we conducted a comprehensive investigation of core proteomics to explore a potential reverse vaccine candidate with high antigenicity. Methods To identify the immunodominant epitopes, T. cruzi core proteomics was initially explored. Consequently, the vaccine sequence was engineered to possess characteristics of non-allergenicity, antigenicity, immunogenicity, and enhanced solubility. After modeling the tertiary structure of the human TLR4 receptor, the binding affinities were assessed employing molecular docking and molecular dynamics simulations (MDS). Results Docking of the final vaccine design with TLR4 receptors revealed substantial hydrogen bond interactions. A server-based methodology for immunological simulation was developed to forecast the effectiveness against antibodies (IgM + IgG) and interferons (IFN-g). The MDS analysis revealed notable levels of structural compactness and binding stability with average RMSD of 5.03 Aring;, beta-factor 1.09e+5 Å, Rg is 44.7 Aring; and RMSF of 49.50 Aring;. This is followed by binding free energies calculation. The system stability was compromised by the complexes, as evidenced by their corresponding Gibbs free energies of -54.6 kcal/mol. Discussion Subtractive proteomics approach was applied to determine the antigenic regions of the T cruzi. Our study utilized computational techniques to identify B- and T-cell epitopes in the T. cruzi core proteome. In current study the developed vaccine candidate exhibits immunodominant features. Our findings suggest that formulating a vaccine targeting the causative agent of Chagas disease should be the initial step in its development.
... We were also interested in learning if these compounds would impart a growth inhibitory effect on T. brucei, the etiological agent of human African trypanosomiasis [31]. (1)(2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13). For systematic names and SMILES codes of the compounds, please refer to Tables S1 and S2 in the Supplementary Information section, respectively. ...
... A cytotoxicity assessment was also performed on the NIH-3T3 fibroblasts. A structure-activity relationship (SAR) analysis was devised to help understand the molecular determinants pertaining to the 3-nitro-2- (1)(2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13). For systematic names and SMILES codes of the compounds, please refer to Tables S1 and S2 in the Supplementary Information section, respectively. ...
Article
Full-text available
Chagas disease is one of the world’s neglected tropical diseases, caused by the human pathogenic protozoan parasite Trypanosoma cruzi. There is currently a lack of effective and tolerable clinically available therapeutics to treat this life-threatening illness and the discovery of modern alternative options is an urgent matter. T. cruzi glucokinase (TcGlcK) is a potential drug target because its product, d-glucose-6-phosphate, serves as a key metabolite in the pentose phosphate pathway, glycolysis, and gluconeogenesis. In 2019, we identified a novel cluster of TcGlcK inhibitors that also exhibited anti-T. cruzi efficacy called the 3-nitro-2-phenyl-2H-chromene analogues. This was achieved by performing a target-based high-throughput screening (HTS) campaign of 13,040 compounds. The selection criteria were based on first determining which compounds strongly inhibited TcGlcK in a primary screen, followed by establishing on-target confirmed hits from a confirmatory assay. Compounds that exhibited notable in vitro trypanocidal activity over the T. cruzi infective form (trypomastigotes and intracellular amastigotes) co-cultured in NIH-3T3 mammalian host cells, as well as having revealed low NIH-3T3 cytotoxicity, were further considered. Compounds GLK2-003 and GLK2-004 were determined to inhibit TcGlcK quite well with IC50 values of 6.1 µM and 4.8 µM, respectively. Illuminated by these findings, we herein screened a small compound library consisting of thirteen commercially available 3-nitro-2-phenyl-2H-chromene analogues, two of which were GLK2-003 and GLK2-004 (compounds 1 and 9, respectively). Twelve of these compounds had a one-point change from the chemical structure of GLK2-003. The analogues were run through a similar primary screening and confirmatory assay protocol to our previous HTS campaign. Subsequently, three in vitro biological assays were performed where compounds were screened against (a) T. cruzi (Tulahuen strain) infective form co-cultured within NIH-3T3 cells, (b) T. brucei brucei (427 strain) bloodstream form, and (c) NIH-3T3 host cells alone. We report on the TcGlcK inhibitor constant determinations, mode of enzyme inhibition, in vitro antitrypanosomal IC50 determinations, and an assessment of structure–activity relationships. Our results reveal that the 3-nitro-2-phenyl-2H-chromene scaffold holds promise and can be further optimized for both Chagas disease and human African trypanosomiasis early-stage drug discovery research.
... 5 Studies of T. sanguisuga in Florida, 6 Texas, 7-9 and Louisiana 10-12 found that the species feeds on humans and multiple animal taxa 9,13,14 in both rural and urban areas. 6,15,16 Trypanosoma cruzi infection prevalences in T. sanguisuga collected in Louisiana and Texas between 2007 and 2016 ranged from 30% to 62%. 8,10,13,17 Triatoma sanguisuga is found in all six states of the Mid-Atlantic (New York, New Jersey, Pennsylvania, Delaware, Maryland, and Virginia) and Washington DC, but little is known of its regional ecology or epidemiology. ...
Article
Full-text available
In July and October 2023, two live triatomine bugs were found inside a home in New Castle County, Delaware. The bugs were identified as Triatoma sanguisuga , the most widespread triatomine bug species in the United States. Triatoma sanguisuga is a competent vector of Trypanosoma cruzi , the causative agent of Chagas disease. The two specimens were tested via real-time PCR (qPCR) for infection with T. cruzi , and one of the specimens was positive. Despite T. sanguisuga being endemic to the area, attainment of accurate species identification and T. cruzi testing of the bugs required multiple calls to federal, state, private, and academic institutions over several months. This constitutes the first report of T. sanguisuga infected with T. cruzi in Delaware. In addition, this is the first published report of T. sanguisuga in New Castle County, the northernmost and most densely populated county in Delaware. New Castle County still conforms to the described geographic range of T. sanguisuga , which spans from Texas to the East Coast of the United States. The T. cruzi infection prevalence of the species has not been studied in the northeastern United States, but collections in southern states have found prevalences as high as 60%. The Delaware homeowner’s lengthy pursuit of accurate information about the vector highlights the need for more research on this important disease vector in Delaware.
... 6,7 In the past years, the prevalence of the disease has dislocated from rural areas to being mostly urban, and globalization combined with intensified people migrations has significantly increased the number of cases in nonendemic areas such as North America, Europe, and Asia. [8][9][10][11] The infective trypomastigote form can penetrate nearly any nucleated cell type, differentiates to round-shaped amastigotes that multiply several times in the cytoplasm before differentiating back to trypomastigotes, which are released in adjacent tissue after host cell rupture to then disseminate through the circulation. 12 Host cell invasion is mediated by a complex and heterogeneous network of parasite and host cell molecules, including the cell surface proteins gp30 and gp82 in metacyclic trypomastigotes (infective form found in the triatomine feces) 13,14 ; while in tissue culture-derived or blood trypomastigotes, gp85, 15,16 transialidase, 17,18 mucins, 19 cruzipain (papain-like protease), [20][21][22] oligopeptidase B (serine peptidase), 23 among many others, have been identified as molecules contributing to host cell invasion. ...
Article
Full-text available
Trypanosoma cruzi is the causative agent of Chagas disease, a chronic pathology that affects the heart and/or digestive system. This parasite invades and multiplies in virtually all nucleated cells, using a variety of host cell receptors for infection. T. cruzi has a gene that encodes an ecotin‐like inhibitor of serine peptidases, ISP2. We generated ISP2‐null mutants (Δisp2) in T. cruzi Dm28c using CRISPR/Cas9. Epimastigotes of Δisp2 grew normally in vitro but were more susceptible to lysis by human serum compared to parental and ISP2 add‐back lines. Tissue culture trypomastigotes of Δisp2 were more infective to human muscle cells in vitro, which was reverted by the serine peptidase inhibitors aprotinin and camostat, suggesting that host cell epitheliasin/TMPRSS2 is the target of ISP2. Pretreatment of host cells with an antagonist to the protease‐activated receptor 2 (PAR2) or an inhibitor of Toll‐like receptor 4 (TLR4) selectively counteracted the increased cell invasion by Δisp2, but did not affect invasion by parental and add‐back lines. The same was observed following targeted gene silencing of PAR2, TLR4 or TMPRSS2 in host cells by siRNA. Furthermore, Δisp2 caused increased tissue edema in a BALB/c mouse footpad infection model after 3 h differently to that observed following infection with parental and add‐back lines. We propose that ISP2 contributes to protect T. cruzi from the anti‐microbial effects of human serum and to prevent triggering of PAR2 and TLR4 in host cells, resulting in the modulation of host cell invasion and contributing to decrease inflammation during acute infection.
... Transmission is caused by the donation of organs infected with T. cruzi, which are transplanted to healthy patients and they develop the disease (Fig. 1b3) [5,10,21]. ...
... Symptomatology can also occur within a few hours or days of birth (fever, general condition involvement and meningoencephalitis) [10, 11,20,21]. Is the third most medically important transmission route in urban areas of Latin America, as well as in non-endemic countries [7,11,12,15]. ...
... Some foods associated with this transmission pathway in South America have been cane juice and acai in Brazil, guava juice in Venezuela and palm wine in Colombia, as well as meat of hunting animals in Argentina and Ecuador [10,12,18,22]. This type of transmission has caused infectious micro-outbreaks in small groups such as families, in schools and in small communities established on the periphery of selvatic ecosystems, where they naturally inhabit infected triatomines and reservoirs [5,7,10,21,22]. ...
Preprint
Full-text available
Chagas disease (Chd) belongs to the group of neglected tropical diseases (NTDs) and is caused by the protozoa Trypanosoma cruzi (T. cruzi) which is transmitted vector mainly by insects from the subfamily Triatominae and said parasitosis affects different mammals, including humans. In addition, Chd is one of the most worrying public health problems in Latin America and progressively with the greatest impact around the world, as a result of a high health, social and economic impact, as well as, by the great lag in an effective therapeutic treatment.
... 5 The natural transmission of Trypanosoma cruzi in the Americas through triatomine insects causes around twelve thousand deaths a year and many babies are born infected. 6 In 1980, Chagas disease was considered one of the five leading causes of morbidity and mortality in the Americas. 7 These diseases, considered forgotten and neglected, have no vaccine available and their control has focused primarily on pharmacological treatment and vector control, due to their difficult social environment and biological complexity; which includes a wide variety of species, complex life cycles, drug resistance, drug toxicity, limited use in pregnant women, high costs, poor availability in endemic places, poorly understood pharmacological mechanisms of action, little investment in development of vaccines and the shortage of drugs in endemic areas to treat these diseases in the last 80 years. ...
Article
Full-text available
Trypanosomatids are an important group of parasites that predominate in tropical and subtropical areas of the planet, which cause diseases that are classified as forgotten and neglected by the world health organization. In this group of parasites, we find Trypanosoma cruzi, Trypanosoma brucei, Trypanosoma brucei rhodesiense and Leishmania spp, for which there is no vaccine available, and its control has focused mainly on pharmacological treatment. Due to the poverty situation where these diseases are found and the biological complexity of these parasites, there are multiple variables to control, including the diversity of species, the complexity of their life cycles, drug resistance, cytotoxicity, the limited use in pregnant women, the high costs of treatment and the little-known pharmacological mechanisms of action, among others. It is therefore necessary to find new strategies and approaches for the treatment of these parasitic diseases. Among these new approaches is the rational search for new targets based on the allosteric inhibition of protein kinases, which have been little studied in trypanosomatids. Among these kinases, we find Glycogen Synthase Kinase-3 (GSK-3), a kinase of great pharmacological interest, which is under intense basic and clinical research by pharmaceutical companies for the treatment of cancer. This kinase, highly studied in the PI3K/AKT/mTOR pathway signaling in humans, has an orthologous gene in these parasites (GSK-3 s), which has proven to be essential for them in response to different challenges; Therefore, it is notable to increase research in this kinase in order to achieve a broad structural and functional characterization in the different species of trypanosomatids. Keywords: Trypanosomatids; GSK-3; Leishmania spp; Trypanosoma cruzi; Trypanosoma brucei; Trypanosoma brucei rhodesiense; PI3K/AKT/mTOR
... Transmission is caused by the donation of organs infected with T. cruzi, which are transplanted to healthy patients and they develop the disease (Fig. 1b3) [5,10,21]. ...
... Symptomatology can also occur within a few hours or days of birth (fever, general condition involvement and meningoencephalitis) [10, 11,20,21]. Is the third most medically important transmission route in urban areas of Latin America, as well as in non-endemic countries [7,11,12,15]. ...
... Some foods associated with this transmission pathway in South America have been cane juice and acai in Brazil, guava juice in Venezuela and palm wine in Colombia, as well as meat of hunting animals in Argentina and Ecuador [10,12,18,22]. This type of transmission has caused infectious micro-outbreaks in small groups such as families, in schools and in small communities established on the periphery of selvatic ecosystems, where they naturally inhabit infected triatomines and reservoirs [5,7,10,21,22]. ...
... Potential conflicts involving opossums include foraging in trash, denning in manmade structures, and nest predation of ground-nesting birds (Clark 1994;Staller et al. 2005). Additionally, opossums may be vectors for diseases such as Chagas disease (Bern et al. 2011;Bernasconi et al. 2023), murine typhus (Civen and Ngo 2008), and bovine tuberculosis (Walter et al. 2013). Opossums are also the definitive hosts to the parasite that causes equine myeloencephalitis, a disease that costs the horse industry millions of dollars annually (Dubey et al. 2001;Dubey and Lindsay 1999). ...
Article
The Virginia opossum (Didelphis virginiana) has a rapidly expanding distribution in North America, but many aspects of its ecology remain relatively understudied, particularly in rural areas of its core range. We collected GPS telemetry data from 93 opossums in a rural, non-agricultural landscape in South Carolina, USA (2018–2019) to examine factors influencing space use and resource selection. Estimated male home ranges (99% utilization distributions) were on average 50% larger than those of females (mean home range 115.9 ± 103.7 ha vs 76.7 ± 75.0 ha). The home range size decreased on average by 20% with each 20% increase in deciduous land cover but was not affected by season or other landscape factors. Core area sizes (65% utilization distributions) were not influenced by sex (mean core area size 29.1 ± 23.7 ha and 22.4 ha ± 13.8 for males and females, respectively) or season, but the core area size decreased by 14% with each 400 m increase in distance from a permanent water source. Resource selection by opossums primarily occurred at the landscape level. Both males and females generally selected for wetlands while avoiding pine forests and developed/open areas, likely the result of differences in resource availability and predation risk between habitats. Opossums also tended to select for linear features such as unpaved roads and edge habitat, which may facilitate movement across the landscape. The home ranges we documented are among the largest recorded for opossums in the USA, likely the result of the relatively low resource abundance throughout our study area due to comparatively minimal anthropogenic influence.
... Due to the sylvatic nature of the 11 triatomine species found in the United States, the geographical ranges of these vectors in the United States have been difficult to elucidate in an efficient and comprehensive way. Historical literature from as early as 1855 (Le Conte 1855) and subsequent work by many researchers and community scientists have slowly pieced together likely ranges of the species found in the United States (Lent and Wygodzinsky 1979, Bern et al. 2011, Zeledón et al. 2012, Curtis-Robles et al. 2018a). The 2 species reported in Illinois and Missouri are Triatoma sanguisuga (the Eastern Bloodsucking Conenose bug) and Triatoma lecticularia (also known as Paratriatoma lecticularia (de Paiva et al. 2021, Bern et al. 2011, McPherson 2017. ...
... Historical literature from as early as 1855 (Le Conte 1855) and subsequent work by many researchers and community scientists have slowly pieced together likely ranges of the species found in the United States (Lent and Wygodzinsky 1979, Bern et al. 2011, Zeledón et al. 2012, Curtis-Robles et al. 2018a). The 2 species reported in Illinois and Missouri are Triatoma sanguisuga (the Eastern Bloodsucking Conenose bug) and Triatoma lecticularia (also known as Paratriatoma lecticularia (de Paiva et al. 2021, Bern et al. 2011, McPherson 2017. Triatoma sanguisuga and T. lecticularia likely have northern range limits in the midwestern US states of Illinois and Missouri (Bern et al. 2011) (Fig. 1). ...
... The 2 species reported in Illinois and Missouri are Triatoma sanguisuga (the Eastern Bloodsucking Conenose bug) and Triatoma lecticularia (also known as Paratriatoma lecticularia (de Paiva et al. 2021, Bern et al. 2011, McPherson 2017. Triatoma sanguisuga and T. lecticularia likely have northern range limits in the midwestern US states of Illinois and Missouri (Bern et al. 2011) (Fig. 1). However, historical literature reveals relatively little about the vector or T. cruzi in these states. ...
Article
Triatomine species (kissing bugs) infected with Trypanosoma cruzi are found across the southern United States. The northern limits of Trypanosoma cruzi infected kissing bugs are less understood. The objective of this work was to describe the locations of kissing bugs from Illinois and Missouri based on historical records, submissions to Texas A&M University’s (TAMU) Kissing Bug Community Science Program and the Centers for Disease Control and Prevention (CDC), and records from online platforms (iNaturalist, BugGuide, and GBIF) up to and including 2022. A total of 228 records were discovered, including 186 from historical or observation platforms and 42 specimens submitted to TAMU or CDC. Species included Triatoma sanguisuga (221 total records, 9 nymphs) and Triatoma lecticularia (7 records). Notably, nearly all (24/26) records submitted to TAMU were collected indoors. Twelve of the 30 (40%) specimens tested were positive for the presence of T. cruzi, including parasite discrete taxonomic units TcI and TcIV. One triatomine sample had been found in a bed feeding on the submitter; this bug was positive for T. cruzi and had evidence of human blood in its gut. Records suggest a ubiquitous distribution in Missouri and potentially to the northernmost border in Illinois. Further investigations into triatomine distribution and infection status are needed within states assumed to be northern limits in order to create public health and veterinary health messaging and baseline distributional maps from which to measure future range shifts in relation to a changing climate.